Captiva Spine Receives 510(k) Clearance for PIVOTEC

Captiva Spine, a medical device organization dedicated to developing and distributing spinal technologies in the United States and internationally, announced that it has received 510(k) clearance for its cutting edge interbody system, the PIVOTEC, according to a Captiva news release.

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PIVOTEC is a transforaminal lumbar interbody fusion technology that addresses the challenge of controlling cage insertion and manipulation during surgery, according to the report. The PIVOTEC system uses an inserter that allows the cage to safely and accurately pivot without disengaging from the instrument.

The PIVOTEC was successfully introduced during the North American Spine Society meeting held in San Francisco in November.

Read the release about the 510(k) clearance for Captiva Spine’s PIVOTEC.

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